The University of Massachusetts Amherst

The Plant Cell Culture Library

Carpesium cernuum
Cell Line ID CC-01071-R1
Media Type B105
Lowest Tolerable USDA Zone 7a
Drought Tolerance Not tolerant
Availability high
Order Asterales
Family Compositae
Genus Carpesium
Antibacterial Genus Level ➡ 19 citations
Anticancer Genus Level
Culture Start Material Shoot
Plant Supplier Botanical Garden Chelsea Physic Garden
Antibacterial Citations
  1. Herz, W. et al., J. Org. Chem., 1966, 31, 3232- 3236; 1982, 47, 3991 - 3993 (Ivaxillin, cryst struct) [https://doi.org/10.1021/jo01348a032]
  2. Torrance, S.J. et al., Phytochemistry, 1969, 8, 2381- 2392 (Eriolin) [https://doi.org/10.1016/S0031-9422(00)88158-3]
  3. Takeda, K. et al., J. Chem. Soc., Perkin Trans. 1, 1975, 870- 876 (synth) [https://doi.org/10.1039/p19750000870]
  4. Ravindranath, K.R. et al., Indian J. Chem., Sect. B, 1978, 16, 27- 31 (Inunolide,Dihydroinunolide)
  5. Bohlmann, F. et al., Phytochemistry, 1978, 17, 1165- 1172 (Inula epoxides) [https://doi.org/10.1016/S0031-9422(00)94308-5]
  6. Brecknell, D.J. et al., Aust. J. Chem., 1979, 32, 2455- 2471 (Callitris columellaris constit) [https://doi.org/10.1071/CH9792455]
  7. Romo de Vivar, A. et al., Phytochemistry, 1982, 21, 2905- 2908 (11,13-Dehydroeriolin) [https://doi.org/10.1016/0031-9422(80)85065-5]
  8. Bohlmann, F. et al., Liebigs Ann. Chem., 1983, 2227- 2246 (Calea szyszylowiczii constit)
  9. Maruyama, M. et al., Phytochemistry, 1983, 22, 2773- 2774 (Eriolin, Ivaxillin, 11,13-Dehydroivaxillin, isol, struct) [https://doi.org/10.1016/S0031-9422(00)97693-3]
  10. Bohlmann, F. et al., Phytochemistry, 1984, 23, 1669- 1672 (Ferreyranthus constit) [https://doi.org/10.1016/S0031-9422(00)83465-2]
  11. Watson, W.H. et al., J. Org. Chem., 1986, 51, 2521- 2524 (struct) [https://doi.org/10.1021/jo00363a022]
  12. Jakupovic, J. et al., Phytochemistry, 1987, 26, 451- 455 (Critonia quadrangularis epoxide) [https://doi.org/10.1016/S0031-9422(00)81431-4]
  13. Calderon, J.S. et al., Phytochemistry, 1987, 26, 1747- 1750 (11,13-Dehydroeriolin, cryst struct) [https://doi.org/10.1016/S0031-9422(00)82281-5]
  14. Hubert, T.D. et al., Phytochemistry, 1987, 26, 1751- 1753 (Quadrangolide) [https://doi.org/10.1016/S0031-9422(00)82282-7]
  15. Zdero, C. et al., Phytochemistry, 1988, 27, 2835- 2842 (Inunolide) [https://doi.org/10.1016/0031-9422(88)80673-3]
  16. Paknikar, S.K. et al., Planta Med., 1988, 54, 186- 187 (struct) [https://doi.org/10.1055/s-2006-962395]
  17. Toyota, M. et al., Phytochemistry, 1991, 30, 563- 573 (Porella acutifolia constit) [https://doi.org/10.1016/0031-9422(91)83728-4]
  18. Bardón, A. et al., Phytochemistry, 1996, 41, 845- 849 (Quadrangolide, pmr, cmr) [https://doi.org/10.1016/0031-9422(95)00691-5]
  19. Cheng, X. et al., Eur. J. Med. Chem., 2011, 46, 5408- 5415 (Inula falconeri constit) [https://doi.org/10.1016/j.ejmech.2011.08.047]
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